Last week, the United States Food and Drug Administration (FDA) and A.P. Deauville issued a voluntary recall for over 67,000 cases of Power Stick deodorant due to “cGMP deviations,” which is a difference in the Current Good Manufacturing Practice regulations the FDA oversees.

The FDA did not provide a reason for the recall, but said the products had a cGMP (Current Good Manufacturing Practices) deviation.

More than 67,000 cases of roll-on deodorant that were sold nationwide have been voluntarily recalled due to an undisclosed manufacturing defect.

Over 67,000 cases of “Power Stick” roll‑on deodorant recalled by A.P. Deauville due to cGMP violations. Three variants are included – Power Stick F

A.P. Deauville recalled over 67,000 cases of Power Stick roll-on deodorants. The recall happened because the products did not follow FDA safety rules. The affected deodorants include Powder Fresh, Spring Fresh,

CHICAGO - A recall is underway for tens of thousands of cases of Power Stick antiperspirant deodorant, according to the FDA; two Chicago women allegedly stole clothes from an Oak Brook store and led police on a high-speed chase; and what started as a playful concert tradition turned into a viral PR nightmare for two tech executives.